Canonical Allele Identifier: PA108855
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50905
ClinVar RCV Id: RCV000043620 RCV000872109 RCV001149870 RCV001149871 RCV002513637
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162580.1:p.Arg114His
CA143840
NM_001169109.2:c.341G>A